De Novo And Inherited Tcf20 Pathogenic Variants Are Associated With Intellectual Disability, Dysmorphic Features, Hypotonia, And Neurological Impairments With Similarities To Smith-Magenis Syndrome (Vol 11, 12, 2019) Francesco Vetrini , Shane Mckee , Jill A. Rosenfeld , Mohnish Suri , Andrea M. Lewis , Kimberly Margaret Nugent , Elizabeth Roeder , Rebecca O. Littlejohn , Sue Holder , Wenmiao Zhu , Joseph T. Alaimo , Brett Graham , Jill M. Harris , James B. Gibson , Matthew Pastore , Kim L. Mcbride , Makanko Komara , Lihadh Al-Gazali , Aisha Al Shamsi , Elizabeth A. Fanning , Klaas J. Wierenga , Daryl A. Scott , Ziva Ben-Neriah , Vardiella Meiner , Hanoch Cassuto , Orly Elpeleg , J. Lloyd Holder , Lindsay C. Burrage , Laurie H. Seaver , Lionel Van Maldergem , Sonal Mahida , Janet S. Soul , Margaret Marlatt , Ludmila Matyakhina , Julie Vogt , June-Anne Gold , Soo-Mi Park , Vinod Varghese , Anne K. Lampe , Ajith Kumar , Melissa Lees , Muriel Holder-Espinasse , Vivienne Mcconnell , Birgitta Bernhard , Ed Blair , Victoria Harrison , Donna M. Muzny , Richard A. Gibbs , Sarah H. Elsea , Jennifer E. Posey , Weimin Bi , Seema Lalani , Fan Xia , Yaping Yang , Christine M. Eng , James R. Lupski , Pengfei Liu GENOME MEDICINE(2019)
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